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Biodegradation of selected xenobiotic compounds: Chlorinated phenols and 2,4,6-trinitrotoluene.

机译:所选异种生物化合物的生物降解:氯化酚和2,4,6-三硝基甲苯。

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Microbial degradation of substituted aromatic compounds was studied under aerobic conditions. Target compounds included, phenol, 2,4-dichlorophenol, pentachlorophenol, and 2,4,6-trinitrotoluene. These compounds tend to inhibit dioxygenase attack of the benzene ring due to the presence of electron-withdrawing characteristics of substituted nitro- or chloro-groups.; Biodegradation of phenolic compounds under multiple substrate conditions revealed significant substrate interactions affecting the growth of the microorganisms. The presence of the growth substrate, phenol, increased the growth of a mixed culture on other chlorinated phenols. After the introduction of chlorinated phenols, a decrease in microbial species diversity was observed resulting in a change of the kinetic constants. The remaining culture had higher substrate affinity, lower growth rate, and was more susceptible to inhibitory effects of chlorinated phenols.; Under carbon and nitrogen limited conditions in fed-batch reactors, the biotransformation of TNT was investigated. Results showed that the rate of intermediates formation depended on the substrate condition. Nine aerobic bacterial species were isolated from a soil contaminated with munitions waste from a site in Illinois. These species were tentatively identified as: one Enterobacter sp., one Pseudomonas sp., and seven Alcaligenes spp.; With two of the best performers out of the nine isolates, the effects of culture conditions on TNT transformation were studied. TNT was transformed faster in the presence of high concentrations of supplemental carbon sources and azoxy-compound formation was minimized by decreasing culture pH. The presence of nitrogen sources in any form did not affect TNT transformation by Alcaligenes sp. I15. However, the presence of a nitrogen source as nitrate significantly inhibited TNT transformation by Enterobacter sp. I5.; Enterobacter sp. I5 mineralized TNT (3.2%) after 10 days of incubation in the respirometer and the result was reproducible. Unknown polar intermediates were identified by GC-MS analysis. New intermediates identified were 4-acetamido-2,6-nitrotoluene, 4-acetamido-2-amino-6-nitrotoluene, 4-amino-2-nitrotoluene, 4-acetamido-2-nitrotoluene, and 3-methylcatechol. Results showed that transformation of TNT by Enterobacter sp. I5 involves a combination of acetylation, reduction, and deamination. Aerobic mineralization of TNT was possible, however, it might be necessary to increase the amount of mineralization by further optimizing culture conditions.
机译:在好氧条件下研究了取代的芳族化合物的微生物降解。目标化合物包括苯酚,2,4-二氯苯酚,五氯苯酚和2,4,6-三硝基甲苯。由于存在取代的硝基或氯基团的吸电子特性,这些化合物倾向于抑制苯环的双加氧酶攻击。在多种底物条件下对酚类化合物的生物降解显示了显着的底物相互作用,影响了微生物的生长。生长底物苯酚的存在增加了混合培养物在其他氯化苯酚上的生长。引入氯代苯酚后,观察到微生物物种多样性下降,导致动力学常数发生变化。剩余的培养物具有较高的底物亲和力,较低的生长速率,并且更容易受到氯化酚的抑制作用。在补料分批反应器中,在碳和氮限制的条件下,研究了TNT的生物转化。结果表明,中间体的形成速率取决于底物条件。从伊利诺伊州一个地点的被弹药废物污染的土壤中分离出九种需氧细菌。暂定这些物种为:1个肠杆菌属,1个假单胞菌属和7个产碱杆菌属。在9个分离株中,有2个表现最佳,研究了培养条件对TNT转化的影响。在高浓度的补充碳源存在下,TNT的转化速度更快,并且通过降低培养液的pH值可以最大程度地减少叠氮化合物的形成。任何形式的氮源的存在都不会影响Alcaligenes sp。的TNT转化。 I15。但是,氮源作为硝酸盐的存在显着抑制了肠杆菌属的TNT转化。 I5。肠杆菌在呼吸计中温育10天后,I5使TNT矿化(3.2%),结果可重复。通过GC-MS分析鉴定了未知的极性中间体。鉴定出的新中间体为4-乙酰氨基-2-,6-硝基甲苯,4-乙酰氨基-2-氨基-6-硝基甲苯,4-氨基-2-硝基甲苯,4-乙酰氨基-2-硝基甲苯和3-甲基邻苯二酚。结果表明肠杆菌属细菌转化TNT。 I5涉及乙酰化,还原和脱氨基的组合。 TNT有氧矿化是可能的,但是可能有必要通过进一步优化培养条件来增加矿化量。

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